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rs267608066

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267608066(C;T)
Make rs267608066(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position47798713
GeneMSH6
is asnp
is mentioned by
dbSNPrs267608066
ebirs267608066
HLIrs267608066
Exacrs267608066
Varsomers267608066
Maprs267608066
PheGenIrs267608066
hapmaprs267608066
1000 genomesrs267608066
hgdprs267608066
ensemblrs267608066
gopubmedrs267608066
geneviewrs267608066
scholarrs267608066
googlers267608066
pharmgkbrs267608066
gwascentralrs267608066
openSNPrs267608066
23andMers267608066
23andMe allrs267608066
SNP Nexus

SNPshotrs267608066
SNPdbers267608066
MSV3drs267608066
GWAS Ctlgrs267608066
Max Magnitude0
ClinVar
Risk rs267608066(T;T)
Alt rs267608066(T;T)
Reference rs267608066(C;C)
Significance Pathogenic
Disease Lynch syndrome
Variation info
Gene MSH6
CLNDBN Lynch syndrome
Reversed 0
HGVS NC_000002.11:g.48025852C>T
CLNSRC International Society for Gastrointestinal Hereditary Tumours
CLNACC RCV000075029.2,